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JCO Precision Oncology|January 7, 2022
Impact of Variant Reclassification in Cancer Predisposition Genes on Clinical CareJianbang Chiang, Tze Hao Chia, Jeanette Yuen, et al.Familial Cancer|May 15, 2020
Biallelic NF1 inactivation in high grade serous ovarian cancers from patients with neurofibromatosis type 1Eliza Courtney, Sock Hoai Chan, Shao Tzu Li, et al.Familial Cancer|February 13, 2020
Missense PALB2 germline variant disrupts nuclear localization of PALB2 in a patient with breast cancerMing Ren Toh, Chen Ee Low, Siao Ting Chong, et al.NPJ Genomic Medicine|October 7, 2020
Multiple neoplasia in a patient with Gitelman syndrome harboring germline monoallelic MUTYH mutationJason Yongsheng Chan, Ming Ren Toh, Siao Ting Chong, et al.Bioinformatics (Oxford, England)|July 26, 2022
Automatic DNA replication tract measurement to assess replication and repair dynamics at the single-molecule levelLongjie Li, Arun Mouli Kolinjivadi, Kok Haur Ong, et al.Journal of Medical Genetics|March 24, 2017
Impact of subsidies on cancer genetic testing uptake in SingaporeShao-Tzu Li, Jeanette Yuen, Ke Zhou, et al.Gynecologic Oncology|January 10, 2016
Mutation spectrum of POLE and POLD1 mutations in South East Asian women presenting with grade 3 endometrioid endometrial carcinomasAdele Wong, Chik Hong Kuick, Wai Loong Wong, et al.International Journal of Cancer|August 4, 2020
Investigation into the origins of an ancient BRCA1 founder mutation identified among Chinese families in SingaporeTarryn Shaw, Sock Hoai Chan, Jing Xian Teo, et al.JNCI Cancer Spectrum|July 31, 2019
Germline Pathogenic Variants in Homologous Recombination and DNA Repair Genes in an Asian Cohort of Young-Onset Colorectal CancerMing Ren Toh, Jian Bang Chiang, Siao Ting Chong, et al.Genome Medicine|January 8, 2021
Family history assessment significantly enhances delivery of precision medicine in the genomics eraYasmin Bylstra, Weng Khong Lim, Sylvia Kam, et al.Pageof 3